Canonical Allele Identifier: CA405462093

Gene: WDR62

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104801C>T , CM000681.2:g.36104801C>T	GRCh38
NC_000019.9:g.36595703C>T , CM000681.1:g.36595703C>T	GRCh37
NC_000019.8:g.41287543C>T	NCBI36
NG_028101.1:g.54921C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4330C>T	ENSP00000270301.6:p.Gln1444Ter
ENST00000401500.7:c.4345C>T MANE Select	ENSP00000384792.1:p.Gln1449Ter
ENST00000587391.6:c.*4205C>T	ENSP00000465525.1:n.*4205C>T
ENST00000679357.1:c.2425C>T
ENST00000679598.1:c.1090C>T
ENST00000679682.1:c.4330C>T	ENSP00000506226.1:p.Gln1444Ter
ENST00000679714.1:c.4339C>T	ENSP00000506627.1:p.Gln1447Ter
ENST00000679757.1:c.3994C>T	ENSP00000505158.1:p.Gln1332Ter
ENST00000679858.1:c.*3727C>T	ENSP00000505655.1:n.*3727C>T
ENST00000680211.1:c.946C>T	ENSP00000506102.1:p.Gln316Ter
ENST00000680280.1:n.1848C>T
ENST00000680349.1:n.2994C>T
ENST00000680403.1:c.*117C>T	ENSP00000505677.1:n.*117C>T
ENST00000680564.1:c.4096C>T	ENSP00000505582.1:p.Gln1366Ter
ENST00000680590.1:c.*2725C>T	ENSP00000505350.1:n.*2725C>T
ENST00000680597.1:c.1078C>T
ENST00000680739.1:c.1360C>T
ENST00000680773.1:n.2846C>T
ENST00000680806.1:c.*3648C>T	ENSP00000506418.1:n.*3648C>T
ENST00000680997.1:n.2277C>T
ENST00000681608.1:n.2190C>T
ENST00000681625.1:c.*1677C>T	ENSP00000505555.1:n.*1677C>T
ENST00000681648.1:n.2396C>T
ENST00000270301.11:c.4330C>T	ENSP00000270301.6:p.Gln1444Ter
ENST00000401500.6:c.4345C>T	ENSP00000384792.1:p.Gln1449Ter
ENST00000587391.5:c.*4205C>T	ENSP00000465525.1:n.*4205C>T
NM_001083961.1:c.4345C>T	NP_001077430.1:p.Gln1449Ter
NM_173636.4:c.4330C>T	NP_775907.4:p.Gln1444Ter
XM_005258809.2:c.4234C>T	XP_005258866.1:p.Gln1412Ter
XM_011526837.1:c.4330C>T	XP_011525139.1:p.Gln1444Ter
XM_011526838.1:c.4096C>T	XP_011525140.1:p.Gln1366Ter
XM_011526839.1:c.3994C>T	XP_011525141.1:p.Gln1332Ter
XM_011526840.1:c.3337C>T	XP_011525142.1:p.Gln1113Ter
XM_011526841.1:c.2923C>T	XP_011525143.1:p.Gln975Ter
XM_011526842.1:c.2776C>T	XP_011525144.1:p.Gln926Ter
XM_011526843.1:c.2092C>T	XP_011525145.1:p.Gln698Ter
XM_011526844.1:c.2092C>T	XP_011525146.1:p.Gln698Ter
XM_011526840.2:c.3337C>T	XP_011525142.1:p.Gln1113Ter
XM_011526841.2:c.2923C>T	XP_011525143.1:p.Gln975Ter
XM_011526844.2:c.2092C>T	XP_011525146.1:p.Gln698Ter
XM_017026665.1:c.4345C>T	XP_016882154.1:p.Gln1449Ter
NM_001083961.2:c.4345C>T MANE Select	NP_001077430.1:p.Gln1449Ter
NM_173636.5:c.4330C>T	NP_775907.4:p.Gln1444Ter